Abstract
Methyl α-isomaltoside and methyl α-isomaltotrioside analogues specifically deoxygenated at position C-2 of various glucopyranosyl units were synthesized by condensation of either 6-O- acetyl-3-O- benzoyl-4-O- benzyl-1-O-tert- butyldimethylsilyl-2-deoxy-β- d-arabino- hexopyranose (trimethylsilyl triflate mediated) or 6-O- acetyl-2,3,4-tri-O- benzyl-α- d-glucopyranosyl chloride (mediated by silver carbonate and silver triflate) with suitably blocked derivatives of methyl α- d-glucopyranoside, its 2-deoxy analogue, or methyl 2′-deoxy-α-isomaltoside.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callDisclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.
